Stannane, dichlorodioctyl-


Chemical Name: Stannane, dichlorodioctyl-
CAS Number: 3542-36-7
Product Number: AG003UF7(AGN-PC-0JLQGQ)
Synonyms:
MDL No:
Molecular Formula: C16H34Cl2Sn
Molecular Weight: 416.0482

Identification/Properties


Properties
MP:
46-48°C
BP:
387.4°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Stability:
Moisture Sensitive
Computed Properties
Molecular Weight:
416.058g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
14
Exact Mass:
416.106g/mol
Monoisotopic Mass:
416.106g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
166
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


NMR Spectrum


Other Analytical Data


Request for Quotation


Customer Feedback


Chemical Structure



Di-n-octyldichlorotin is a versatile organotin compound commonly used in chemical synthesis as a catalyst and reagent. Its primary application lies in the field of organic chemistry, where it acts as a valuable tool for various transformations and reactions.One key application of Di-n-octyldichlorotin is in the catalysis of carbon-carbon bond forming reactions, such as the Stille coupling and Sonogashira coupling. These reactions are crucial in the synthesis of complex organic molecules and are widely used in pharmaceutical, agrochemical, and materials science research.Additionally, Di-n-octyldichlorotin can function as a Lewis acid catalyst in a diverse range of transformations, including Diels-Alder reactions, aldol condensations, and Friedel-Crafts acylations. Its ability to activate and coordinate with a variety of functional groups makes it a valuable asset in designing and optimizing synthetic routes.Furthermore, Di-n-octyldichlorotin can serve as a reagent for the synthesis of organotin compounds, which find application in polymer chemistry, catalysis, and materials science. Its controlled reactivity and compatibility with a wide range of functional groups make it a sought-after compound in organic synthesis laboratories.Overall, Di-n-octyldichlorotin plays a crucial role in facilitating complex chemical transformations and enabling the streamlined synthesis of intricate organic molecules, making it a valuable asset for chemists and researchers engaged in the field of chemical synthesis.